The following data is part of a premarket notification filed by Advanced Instrument Development, Inc. with the FDA for Conversion Contractor Timer Kit.
Device ID | K791933 |
510k Number | K791933 |
Device Name: | CONVERSION CONTRACTOR TIMER KIT |
Classification | Generator, High-voltage, X-ray, Diagnostic |
Applicant | ADVANCED INSTRUMENT DEVELOPMENT, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | IZO |
CFR Regulation Number | 892.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-09-27 |
Decision Date | 1979-11-13 |